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本文引用的文献

1
Interactions between mRNA export commitment, 3'-end quality control, and nuclear degradation.信使核糖核酸输出承诺、3' 端质量控制与核降解之间的相互作用。
Mol Cell Biol. 2002 Dec;22(23):8254-66. doi: 10.1128/MCB.22.23.8254-8266.2002.
2
Stable mRNP formation and export require cotranscriptional recruitment of the mRNA export factors Yra1p and Sub2p by Hpr1p.稳定的mRNA核糖核蛋白(mRNP)形成和输出需要Hpr1p在转录过程中募集mRNA输出因子Yra1p和Sub2p。
Mol Cell Biol. 2002 Dec;22(23):8241-53. doi: 10.1128/MCB.22.23.8241-8253.2002.
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TREX is a conserved complex coupling transcription with messenger RNA export.转录-输出衔接复合体(TREX)是一种保守的复合体,它将转录与信使核糖核酸输出相偶联。
Nature. 2002 May 16;417(6886):304-8. doi: 10.1038/nature746. Epub 2002 Apr 28.
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A conserved mRNA export machinery coupled to pre-mRNA splicing.一种与前体mRNA剪接相关的保守的mRNA输出机制。
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The yin and yang of the exosome.外泌体的阴阳学说。
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The DECD box putative ATPase Sub2p is an early mRNA export factor.DECD盒假定ATP酶Sub2p是一种早期mRNA输出因子。
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Quality control of mRNA 3'-end processing is linked to the nuclear exosome.mRNA 3'端加工的质量控制与核外切体相关。
Nature. 2001 Oct 4;413(6855):538-42. doi: 10.1038/35097110.
8
Box C/D small nucleolar RNA trafficking involves small nucleolar RNP proteins, nucleolar factors and a novel nuclear domain.C/D 盒小核仁RNA转运涉及小核仁核糖核蛋白、核仁因子和一个新的核结构域。
EMBO J. 2001 Oct 1;20(19):5480-90. doi: 10.1093/emboj/20.19.5480.
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Messenger RNAs are recruited for nuclear export during transcription.信使核糖核酸在转录过程中被招募用于核输出。
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10
A block to mRNA nuclear export in S. cerevisiae leads to hyperadenylation of transcripts that accumulate at the site of transcription.酿酒酵母中mRNA核输出的阻断会导致在转录位点积累的转录本发生超腺苷酸化。
Mol Cell. 2001 Apr;7(4):887-98. doi: 10.1016/s1097-2765(01)00232-5.

酿酒酵母中核保留mRNA的定位

Localization of nuclear retained mRNAs in Saccharomyces cerevisiae.

作者信息

Thomsen Rune, Libri Domenico, Boulay Jocelyne, Rosbash Michael, Jensen Torben Heick

机构信息

Department of Molecular Biology, Aarhus University, 8000 Aarhus C., Denmark.

出版信息

RNA. 2003 Sep;9(9):1049-57. doi: 10.1261/rna.5170303.

DOI:10.1261/rna.5170303
PMID:12923254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1370470/
Abstract

In the yeast Saccharomyces cerevisiae, a common conditional phenotype associated with deletion or mutation of genes encoding mRNA export factors is the rapid accumulation of mRNAs in intranuclear foci, suggested to be near transcription sites. The nuclear RNA exosome has been implicated in retaining RNAs in these foci; on deletion of the exosome component Rrp6p, the RNA is released. To determine the exact nuclear location of retained as well as released mRNAs, we have used mRNA export mutant strains to analyze the spatial relationship between newly synthesized heat shock mRNA, the chromosomal site of transcription, and known S. cerevisiae nuclear structures such as the nucleolus and the nucleolar body. Our results show that retained SSA4 RNA localizes to an area in close proximity to the SSA4 locus. On deletion of Rrp6p and release from the genomic locus, heat shock mRNAs produced in the rat7-1 strain colocalize predominantly with nucleolar antigens. Bulk poly(A)(+) RNA, on the other hand, is localized primarily to the nuclear rim. Interestingly, the RNA binding nucleocytoplasmic shuttle protein Npl3p shows strong colocalization with bulk poly(A)(+) RNA, regardless of its nuclear location. Taken together, our data show that retention occurs close to the gene and indicate distinct nuclear fates of different mRNAs.

摘要

在酿酒酵母中,与编码mRNA输出因子的基因缺失或突变相关的一种常见条件表型是mRNA在核内聚集体中快速积累,这些聚集体被认为靠近转录位点。核RNA外切体被认为与RNA在这些聚集体中的保留有关;外切体组分Rrp6p缺失时,RNA会被释放。为了确定保留的和释放的mRNA的确切核定位,我们使用mRNA输出突变菌株来分析新合成的热休克mRNA、转录染色体位点以及酿酒酵母已知的核结构(如核仁与核仁体)之间的空间关系。我们的结果表明,保留的SSA4 RNA定位于与SSA4基因座紧邻的区域。在Rrp6p缺失并从基因组位点释放后,在rat7 - 1菌株中产生的热休克mRNA主要与核仁抗原共定位。另一方面,大量的聚腺苷酸(poly(A))RNA主要定位于核边缘。有趣的是,RNA结合核质穿梭蛋白Npl3p与大量的聚腺苷酸(poly(A))RNA表现出强烈的共定位,无论其在核内的位置如何。综合来看,我们的数据表明RNA保留发生在基因附近,并表明不同mRNA在核内有不同的命运。